Fabersanitas, S.A.
SpainFDA 510(k) applicant, unverified
- Devices
- 3
What Fabersanitas, S.A. makes
Fabersanitas, S.A. manufactures sterile, single-use syringes in two-piece and three-piece configurations, along with sterile disposable needles designed for medical and clinical applications.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These items are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device regulations.
Catalogue
Sterile Disposable Syringes(2 Pieces) Ref K852818
510(k) 510(k)Sterile, Disposable Needle Ref K852817
510(k) 510(k)Sterile Disposable Syringe(3 Pieces) Ref K852819
510(k) 510(k)
Frequently asked questions
How many devices does Fabersanitas, S.A. have in the registry?
The registry currently lists 3 devices for Fabersanitas, S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fabersanitas, S.A.'s devices?
Among its 3 most recently registered devices, Fabersanitas, S.A. has devices listed in FDA 510(k) (3 devices).
What risk classes do Fabersanitas, S.A.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Fabersanitas, S.A.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fabersanitas, S.A. in the registry?
The most recently registered devices listed for Fabersanitas, S.A. include STERILE DISPOSABLE SYRINGES(2 PIECES), STERILE, DISPOSABLE NEEDLE and STERILE DISPOSABLE SYRINGE(3 PIECES).